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RAB39B mutations are a rare finding in Parkinson disease patients

Tobias Löchte, Norbert Brüggemann, Eva Juliane Vollstedt, Patricia Krause, Aloysius Domingo, Raymond Rosales, Lillian V. Lee, Franziska Hopfner, Ana Westenberger, Andrea Kühn, Christine Klein, Katja Lohmann*

*Corresponding author for this work
Original languageEnglish
JournalParkinsonism and Related Disorders
Volume23
Pages (from-to)116-117
Number of pages2
ISSN1353-8020
DOIs
Publication statusPublished - 01.01.2016

Funding

A.A.K. and P.K. are supported by the German Research Foundation (KFO247). N.B. is supported by the Collaborative Center for X-Linked Dystonia-Parkinsonism. A.D. receives a stipend from the German Academic Exchange Service (DAAD). L.V.L. is funded by the Collaborative Center for XDP based at MGH, Boston. C.K. is a recipient of a career development award from the Herman and Lilly Schilling Foundation. K.L. receives research support from the German Research Foundation (DFG; LO 1555/3-2, 1555/8-1).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 10 - Reduced Inequalities
    SDG 10 Reduced Inequalities

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